Export 31 results:
Autore Titolo Tipo [ Anno(Asc)]
Filtri: Autore è Crovella, S  [Clear All Filters]
2015
Rabelo KCN, Albuquerque CMR, Tavares VB, Santos SM, Souza CA, Oliveira TC, Oliveira NCL, Crovella S. Trace samples of human blood in mosquitoes as a forensic investigation tool. Genet Mol Res 2015;14(4):14847-56.
Maranhão RM de Albuq, Esteves FAMartins, Crovella S, Segat L, Souza PREleutér. Tumor necrosis factor-α and interleukin-6 gene polymorphism association with susceptibility to celiac disease in Italian patients. Genet Mol Res 2015;14(4):16343-52.
Barrani M, Massei F, Scaglione M, Paolicchi A, Vitali S, Ciancia EM, Crovella S, Caparello MC, Consolini R. Unusual onset of a case of chronic recurrent multifocal osteomyelitis. Pediatr Rheumatol Online J 2015;13(1):60.
2014
Pellegrin MC, Matarazzo L, Neri E, Pennesi M, Crovella S. HLA-B35, a common genetic trait, in a familial case of Henoch-Schoenlein purpura and Berger's disease. Genet Mol Res 2014;13(2):2669-73.
Segat L, Zupin L, Kim H-Y, Catamo E, Thea DM, Kankasa C, Aldrovandi GM, Kuhn L, Crovella S. HLA-G 14 bp deletion/insertion polymorphism and mother-to-child transmission of HIV. Tissue Antigens 2014;83(3):161-7.
Catamo E, Addobbati C, Segat L, T Fragoso S, A Barbosa D, A Dantas T, H Mariz deAtaíde, da Rocha LF, Duarte ALBranco P, Monasta L, Sandrin-Garcia P, Crovella S. HLA-G gene polymorphisms associated with susceptibility to rheumatoid arthritis disease and its severity in Brazilian patients. Tissue Antigens 2014;84(3):308-15.
Lenarduzzi S, Morgutti M, Crovella S, Coiana A, Rosatelli MC. Short communication: novel truncating mutations in the CFTR gene causing a severe form of cystic fibrosis in Italian patients. Genet Mol Res 2014;13(4):9636-41.
2013
Girardelli M, Bianco AM, Marcuzzi A, Crovella S. A comparative analysis of serologic parameters and oxidative stress in osteoarthritis and rheumatoid arthritis: reply to Mishra and colleagues. Rheumatol Int 2013;33(9):2445-6.
2012
Filho CB, Rodrigues FF, Segat L, Fonseca AM, Araujo J, Arahata C, Pontes L, Vilar L, Filho JL de Lima, Crovella S. Association of MBL2 gene exon 1 variants with autoimmune thyroid disease in Brazilian patients. Int J Immunogenet 2012;39(4):357-61.
Catamo E, Segat L, Lenarduzzi S, Petix V, Morgutti M, Crovella S. CD14 polymorphisms correlate with an augmented risk for celiac disease in Italian patients. Genes Immun 2012;13(6):489-95.
da Silva MFPTBald, Guimarães V, Silva MAR, Amaral CMMedeiros, Beçak W, Stocco RC, Freitas AC, Crovella S. Frequency of human papillomavirus types 16, 18, 31, and 33 and sites of cervical lesions in gynecological patients from Recife, Brazil. Genet Mol Res 2012;11(1):462-6.
Sandrin-Garcia P, Brandão LAC, Guimarães RL, Pancoto JAT, Donadi EA, de Lima-Filho JL, Segat L, Crovella S. Functional single-nucleotide polymorphisms in the DEFB1 gene are associated with systemic lupus erythematosus in Southern Brazilians. Lupus 2012;21(6):625-31.

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